HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880438Generated: October 30, 2026
Ethanol → Ethyl 4-phenyl-1H-pyrrole-2-carboxylate
https://huagongshe.com/reaction/880438
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Glycine methyl ester hydrochloride | HCID 122755 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (3-Dimethylamino-2-phenyl-prop-2-enylidene)-dimethyl-ammonium perchlorate | HCID 78294239 | — |
| Product | Ethyl 4-phenyl-1H-pyrrole-2-carboxylate | HCID 14643813 | 57% |
Reaction Steps
Sodium metal (900 mg, 41.0 mmol) was added to dry ethanol (150 mL) and allowed to dissolve over 30 min. Glycine methyl ester hydrochloride (3.2 g, 25.0 mmol) and (3-dimethylamino-2-phenyl-prop-2-enylidene)-dimethyl-ammonium perchlorate (5.0 g, 16.0 mmol) were added successively and the reaction mixture heated at reflux for 16 h. Ethanol was evaporated in vacuo, the residue diluted with water and extracted with chloroform. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product obtained was purified by column chromatography over neutral alumina using 10% ethyl acetate in petroleum ether as eluent to afford ethyl 4-phenyl-1H-pyrrole-2-carboxylate (2.0 g, 57%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993574B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6fd970e7f2bd41ccac97e96abe1565e9 |
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| Source note | uspto-grants-2015_03 |
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